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HRID 244635Erstellt: 23. Oktober 2026

Diisopropylethylamine → N-(6-bromo-1H-indazol-4-yl)-2-methyl-1,3-thiazole-4-carboxamide

https://huagongshe.com/de/reaction/244635

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-Methyl-1,3-thiazole-4-carboxylic acidHCID 284728—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt6-Bromo-1H-indazol-4-amineHCID 24728063—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(6-bromo-1H-indazol-4-yl)-2-methyl-1,3-thiazole-4-carboxamideHCID 5825575018,9%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

2-Methyl-1,3-thiazole-4-carboxylic acid (4.59 g) (available from Maybridge), HATU (13.41 g) and DIPEA (16.80 ml) were stirred in DMF (140 ml) for 30 min at 20° C. 6-Bromo-1H-indazol-4-amine (3.4 g) (available from Sinova) was added and the reaction stirred at 20° C. for 2 days. The solvent was reduced to ˜40 ml and the reaction mixture was applied across 5×70 g aminopropyl SPE cartridges and left to stand for 3 h. The cartridges were eluted with DCM:methanol (1:1) and the combined solvent was evaporated in vacuo. The residue was suspended in DCM:methanol, adsorbed onto Florisil® and purified by chromatography on silica gel (100 g cartridge) eluting with 0-15% gradient of methanol (containing 1% triethylamine) in DCM over 60 min to give title compound (1.02 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658635B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-a9afde083cea40e7829cf979ee997c21
Quellennotizuspto-grants-2014_02